A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696191



Internal ID15432843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:85752298..85941203hg38UCSC Ensembl
Innerchr7:85381614..85570519hg19UCSC Ensembl
Innerchr7:85219550..85408455hg18UCSC Ensembl
Innerchr7:85026265..85215170hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38188906
hg19188906
hg18188906
hg17188906
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518741
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696191
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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